Search

everythinglearnresearchcommunity

for

Search:↓

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

ZIP10 is crucial for skin development and maintaining healthy skin.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Granzyme B accelerates skin aging and impairs healing by breaking down important skin components.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Using special RNA to target a mutant gene fixed hair problems in mice.

miR-144-y and FOXO3 play key roles in skin and feather development in Zhedong White geese.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Blocking a specific receptor slows down hair loss in mice.

Keratin 17 is crucial for early hair strength and cell survival.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A specific gene mutation causes complete hair loss without other health issues.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Dlx3 is essential for hair growth and regeneration.